J. Plaschke

发表

Nanoscale palladium metallization of DNA

Wolfgang Pompe, Michael Mertig, R. Kirsch, 2000 .

BRCA2germline mutations among early onset breast cancer patients unselected for family history of the disease

J. Chang-Claude, C. Jacobi, H. Schackert, 2000, Journal of medical genetics.

N-Acetyltransferase (NAT) 2 acetylator status and age of tumour onset in patients with sporadic and familial, microsatellite stable (MSS) colorectal cancer

C. Engel, H. Schackert, H. Saeger, 2006, International Journal of Colorectal Disease.

The relationships between the dwarfing genes of wheat and rye

V. Korzun, A. Börner, A. Worland, 2004, Euphytica.

Occult endometrial cancer and decision making for prophylactic hysterectomy in hereditary nonpolyposis colorectal cancer patients.

H. Schackert, H. Saeger, W. Distler, 2006, Gynecologic oncology.

DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2.

T. Meitinger, H. Schackert, W. Ballhausen, 2001, Journal of biochemical and biophysical methods.

Mapping the GA3-insensitive dwarfing gene ct1 on chromosome 7 in rye

V. Korzun, A. Börner, R. Koebner, 1995 .

The putative tumor suppressor gene FHIT at 3p14.2 is rarely affected by loss of heterozygosity in primary human brain tumors.

G. Schackert, H. Schackert, J. Plaschke, 1997, Cancer research.

Quantitative Differences between Aberrant Transcripts Which Occur as Common Isoforms and due to Mutation-based Exon Skipping of the Mismatch Repair Gene hMLH1

H. Schackert, H. Saeger, J. Plaschke, 1999, Clinical chemistry and laboratory medicine.

Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer

M. Kloor, M. Loeffler, P. Kienle, 2006, International journal of cancer.

Evidence that TSG101 aberrant transcripts are PCR artifacts.

G. Schackert, H. Schackert, H. Saeger, 1998, Biochemical and biophysical research communications.

Doublex sequencing in molecular diagnosis of hereditary diseases.

W. Ansorge, H. Schackert, H. Voss, 1998, BioTechniques.

Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer

J. Rüschoff, H. Schackert, R. Fishel, 2000, International journal of cancer.

A microsatellite map of wheat.

M. Ganal, M. Tixier, M. Röder, 1998, Genetics.

Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor

M. Kloor, D. Aust, J. Gebert, 2006, European Journal of Human Genetics.

TCF-3, 4 protein expression correlates with β-catenin expression in MSS and MSI-H colorectal cancer from HNPCC patients but not in sporadic colorectal cancers

H. Schackert, S. Krüger, P. Baláž, 2010, International Journal of Colorectal Disease.

Detection of genetic diversity in closely related bread wheat using microsatellite markers

M. Ganal, M. Röder, J. Plaschke, 1995, Theoretical and Applied Genetics.

Abundance, variability and chromosomal location of microsatellites in wheat

S. Tanksley, M. Ganal, M. Sorrells, 1995, Molecular and General Genetics MGG.

Molecular Mechanisms Associated with Chromosomal and Microsatellite Instability in Sporadic Glioblastoma multiforme

R. Martínez, G. Schackert, H. Schackert, 2004, Oncology.

Low-level microsatellite instability phenotype in sporadic glioblastoma multiforme

H. Schackert, G. Baretton, G. Schackert, 2005, Journal of Cancer Research and Clinical Oncology.

Combined molecular and clinical approach for decision making for surgery in HNPCC patients: a report on three cases in two families

H. Schackert, H. Saeger, J. Plaschke, 2001, International Journal of Colorectal Disease.

Differences in recombination frequency during male and female gametogenesis in rye, Secale cereale L.

V. Korzun, A. Börner, R. Koebner, 1996 .

Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations.

C. Engel, H. Schackert, H. Saeger, 2007, Cancer letters.

Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue

C. Sutter, G. Evans, J. Gebert, 2004, Human mutation.

Genomic rearrangements of hMSH6 contribute to the genetic predisposition in suspected hereditary non-polyposis colorectal cancer syndrome

J. Rüschoff, H. Schackert, J. Plaschke, 2003, Journal of medical genetics.

An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer.

H. Schackert, H. Saeger, R. Koch, 1997, European journal of cancer.

The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC)

M. von Knebel Doeberitz, K. Schulmann, C. Engel, 2005, Journal of Medical Genetics.

Pleiotropic Effects of Genes for Reduced Height (Rht) and Day‐Length Insensitivity (Ppd) on Yield and its Components for Wheat Grown in Middle Europe

A. Börner, C. N. Law, A. Worland, 1993 .

RFLP mapping of genes affecting plant height and growth habit in rye

A. Börner, R. Koebner, M. Gale, 1993, Theoretical and Applied Genetics.

Identification of microsatellite instability and mismatch repair gene mutations in breast cancer cell lines

Susanne Seitz, Uwe Karsten, P. Schlag, 2003, Genes, chromosomes & cancer.

Loss of MSH3 Protein Expression Is Frequent in MLH1-Deficient Colorectal Cancer and Is Associated with Disease Progression 1

Stefan Krüger, Franz Theissig, Giancarlo Marra, 2004, Cancer Research.

Meta- and pooled analyses of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and colorectal cancer: a HuGE-GSEC review.

L. Marchand, L. Le Marchand, V. Moreno, 2009, American journal of epidemiology.

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium.

M. von Knebel Doeberitz, M. Loeffler, J. Gebert, 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Methylenetetrahydrofolate reductase polymorphisms and risk of sporadic and hereditary colorectal cancer with or without microsatellite instability.

H. Schackert, H. Saeger, J. Plaschke, 2003, Cancer letters.

The use of wheat aneuploids for the chromosomal assignment of microsatellite loci

M. Ganal, A. Börner, M. Röder, 2004, Euphytica.

[Molecular pathology in hereditary colorectal cancer. Recommendations of the Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)].

M. Kloor, D. Aust, C. Poremba, 2004, Der Pathologe.

Aberrant protein expression and frequent allelic loss of MSH3 in colorectal cancer with low-level microsatellite instability

A. Ziegler, H. Schackert, J. Plaschke, 2012, International Journal of Colorectal Disease.

Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation

H. Schackert, F. Theissig, H. Saeger, 2002, International journal of cancer.

Identification of six novel MSH2 and MLH1 germline mutations in HNPCC

D. Aust, H. Schackert, F. Theissig, 2003, Human mutation.

Clinical consequences of molecular diagnosis in families with mismatch repair gene germline mutations

H. Schackert, H. Saeger, J. Plaschke, 2000, International Journal of Colorectal Disease.

Microsatellite instability and loss of heterozygosity in squamous cell carcinoma of the head and neck

K. Friedrich, U. Eckelt, J. Plaschke, 2008, Head & neck.

A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8

C. Beetz, J. Plaschke, P. Zacher, 2014, Journal of the Neurological Sciences.

Mlh1-deficient Colorectal Cancer and Is Associated with Loss of Msh3 Protein Expression Is Frequent in Cited Articles Citing Articles E-mail Alerts Loss of Msh3 Protein Expression Is Frequent in Mlh1-deficient Colorectal Cancer and Is Associated with Disease Progression 1

H. Schackert, F. Theissig, H. Saeger, 2004 .

A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression.

T. Wieland, T. Strom, L. Schöls, 2014, European journal of medical genetics.

Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer.

C. Engel, J. Rüschoff, H. Schackert, 2006, Cancer letters.

Absence of Association between Cyclin D 1 ( CCND 1 ) G 870 A Polymorphism and Age of Onset in Hereditary Nonpolyposis Colorectal Cancer

Christoph, Mangold, J. Rüschoff, 2022 .

Ten novel MSH2 and MLH1 germline mutations in families with HNPCC

D. Aust, H. Schackert, H. Saeger, 2004, Human mutation.

Seven novel MLH1 and MSH2 germline mutations in hereditary nonpolyposis colorectal cancer

H. Schackert, F. Theissig, H. Saeger, 2002, Human mutation.

Microsatellite instability and loss of heterozygosity in squamous cell carcinoma of the head and neck

K. Friedrich, U. Eckelt, J. Plaschke, 2008, Head & neck.

Meta- and pooled analyses of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and colorectal cancer: a HuGE-GSEC review.

L. Marchand, C. Wolf, T. Keku, 2009, American journal of epidemiology.